FDA Inspection 1050362 — Omron Healthcare Co., Ltd.
The FDA completed an inspection of Omron Healthcare Co., Ltd. on Feb 27, 2018 in Muko. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Feb 27, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Muko (Japan)